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Journal of Endocrinological Investigation  (0)

A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes Familial Hyperaldosteronism type I

2. CA Carvajal, CB Stehr, PA González, EM Riquelme, T Montero, MJ. Santos,AM. Kalergis and CE. Fardella